Canonical Allele Identifier: CA2200883013

Gene: HBA1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.176983C= , CM000678.2:g.176983C=	GRCh38
NC_000016.9:g.226982C= , CM000678.1:g.226982C=	GRCh37
NC_000016.8:g.166982C=	NCBI36
NG_000006.1:g.37846C=
NG_059186.1:g.5333C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000320868.9:c.150C= MANE Select	ENSP00000322421.5:p.Ser50=
ENST00000397797.1:c.54C=	ENSP00000380899.1:p.Ser18=
ENST00000472694.1:n.286C=
ENST00000487791.1:n.119C=
NM_000558.4:c.150C=	NP_000549.1:p.Ser50=
NM_000558.5:c.150C= MANE Select	NP_000549.1:p.Ser50=